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The Use of Thromboelastography for Assessment of Coagulopathy in Non-trauma Critically Ill Patients. Presenter : Samid M Farooqui M.D PGY2, Department of Internal Medicine Oklahoma University of Health Sciences Center

Transcript of The Use of Thromboelastography for Assessment of ... · The Use of Thromboelastography for...

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The Use of Thromboelastography for Assessment of Coagulopathy in Non-trauma Critically Ill Patients.

Presenter :

Samid M Farooqui M.D

PGY2, Department of Internal Medicine

Oklahoma University of Health Sciences Center

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Disclosure Statement

• I, Samid M Farooqui, have no financial disclosures that would be a potential

conflict of interest with this presentation.

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Background

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• TEG provides a graphical representation of the viscoelastic changes that occur

during the fibrin polymerization process1.

• It evaluates the whole mechanics of clot formation and provides a better

understanding about the interaction between plasma components and cellular

components during clot formation.

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• TEG gives a functionally relevant insight into the coagulation status of critically ill

patients.

• TEG scans are used to guide transfusion in trauma patients and multiple studies

have been done to validate it’s use in trauma patients2,3

• Tartamella F et al.4 reported Thrombodynamic ratio to be an independent

predictor of the odds of thrombosis in critically ill patients.

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Objective

• To determine the utility of TEG scans in the assessment of coagulopathy and risk

of bleeding in non-trauma, critically ill patients. .

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METHODOLOGY

• Critically-ill patients admitted to the medical ICU with abnormalities in standard

coagulation panel.

• Comparison between patients with normal vs. abnormal TEG panel.

• Retrospective cohort analysis.

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• Primary outcome: Development of a bleeding-related event (composite of major

bleed, drop in hemoglobin or need for PRBCs transfusion)

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• Inclusion Criteria

Critically Ill adult patients with an abnormal DIC panel.

• Exclusion Criteria

Patients bleeding on admission

Patients receiving anti-coagulation on admission

Patients who received blood products before TEG scan analysis.

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RESULTS

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Relative risk = 2.15 (CI 1.0-4.62)

p = 0.0377

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RR = 1.07

p = 0.6733

RR = 1.88

p = 0.17

RR = 2.69

p = 0.0157

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DISCUSSION

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• Abnormal TEG cohort had a higher incidence of bleeding-related events.

• A significantly higher number of patients in the abnormal TEG cohort required

transfusion of PRBCs.

• There seems to be a trend towards a higher need of blood products in the

abnormal TEG cohort.

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CONCLUSION

• There is a difference between the incidence of clinically significant bleed and TEG

(normal or abnormal).

• Patients with abnormal TEGs require more PRBC transfusions than those with

normal TEGs.

• Lloyd-Donald et al 5 compared TEG scans in acutely ill Chronic Liver Disease

patients with TEG scans from normal patients and concluded that there was

“delayed clot formation and weaker thrombus strength despite decreased clot

lysis”.

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LIMITATIONS

• Single center

• Retrospective data

• Small sample size

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Future directions

• Prospective analysis

• Data in patients with chronic liver disease

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Acknowledgements

• Dr. Roberto J. Bernardo

• Dr. Ahmed A. Awab

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References

1. R.J.Luddington, Thromboelastography/thromboelastometry. Clin. Lab. Haem 2005, 27,

81-90.

2. Cotton BA et al. Rapid thrombelastography delivers real-time results that predict

transfusion within 1 hour of admission. J Trauma 2011 Aug;71(2):407-14.

3. Holcomb et al. Admission rapid thrombelastography can replace conventional

coagulation tests in the emergency department: experience with 1974

consecutive trauma patients. Ann Surg 2012 Sep;256(3):476-86.

4. Tartamella F, Vasallo MC, Berlot G, Grassi P, Testa F. Thromboelastographic predictors

of venous thromboembolic events in critically ill patients: are we missing something?

Blood Coagul Fibrinolysis. 2016 Oct;27(7):804-811.

5. Lloyd-Donald P et al. Coagulation in acutely ill patients with severe chronic liver disease:

Insights from thromboelastography. J Crit Care. 2017 Apr;38:215-224.